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Dengue Fever 
Jasmial Nand 
Paediatrics 
2014
Outline 
1. References 
2. Introduction 
3. Pathogenesis 
4. Classification 
5. Clinical Course 
6. Assessment 
7. Investigations 
8. Differentials 
9. Management 
10. Additional Points 
11. References
1. References 
ā€¢ Medscape 
ā€¢ Up-to-Date 
ā€¢ WHO Publication 
ā€¢ Dengue Case Management 
ā€¢ CWM ED CME Presentation 
ā€¢ Journal articles 
ā€¢ Tropical Medicine and Intā€™ Health (2001, 2004) 
ā€¢ Indian Journal of Pediatrics (2006) 
ā€¢ Clinical Microbiology Review (2009)
2. Introduction 
ā€¢ The most common arbovirus globally 
ā€¢ Tropics at risk (approx. 2.5-3 Billion) 
ā€¢ 4 distinct serotypes (1-4) 
ā€¢ Flavivirus (ss RNA) 
ā€¢ Vector-borne (Genus Aedes) but other routes possible 
ā€¢ Common species are aegypti, albopictus and 
polynesiensis. 
ā€¢ Transmission/ Outbreak patterns 
ā€¢ Usually self limiting, MR <1%,
3. Pathogenesis 
Martina B E E et al. 
Clin. Microbiol. Rev. 
2009;22:564-581
4. Classification 
Infection 
Asymptomatic Symptomatic 
Undifferentiated Dengue Fever 
NO Warning 
Signs 
Severe Dengue 
With Warning 
Signs 
50-90%
4. Classification (II) 
ā€¢ Dengue fever without warning signs 
ā€¢ Hx of being in endemic area. 
ā€¢ Fever and 2 of the following 
ā€¢ Aches and pains 
ā€¢ Nausea & vomitting 
ā€¢ Rash 
ā€¢ Tourniquet test positive 
ā€¢ Leukopenia
4. Classification (III) 
ā€¢ Dengue with Warning signs 
ā€¢ Fluid accumulation clinically (ascitis, pleural effusion) 
ā€¢ Liver enlargement 
ā€¢ Lethargy (or restlessness) 
ā€¢ Lab (High HCT &/or Low PLT) 
ā€¢ Abdominal pain (or tenderness) 
ā€¢ Vomiting (persistent) 
ā€¢ Insignificant bleeding (Mucosal bleeding) 
ā€œFlaviā€
4. Classifications (IV) 
ā€¢ Severe Dengue 
1. Severe plasma leakage leading to 
ā€¢ Shock 
ā€¢ Fluid accumulation with respiratory distress 
2. Severe bleeding as evidenced by a doctor 
3. Severe organ involvement 
ā€¢ Liver: AST or ALT >1000 
ā€¢ CNS: Impaired consciousness 
ā€¢ Heart and other organ dysfunctions
5. Clinical Course 
ā€¢ Incubation period (3-7 days) 
ā€¢ Febrile phase (2-7 days) 
ā€¢ Critical phase (1-3 days) 
ā€¢ Marked by defervescence , leukopenia and 
thrombocytopenia. 
ā€¢ Recovery phase (or Severe Dengue.) 
ā€¢ May have bradycardia. Important to avoid fluid 
overload! 
ā€¢ Patients can and will present in any of the 3 stages so good 
history and timeline is critical to know where the patient 
stands and what to expect next.
5. Clinical Course (II) 
ā€¢ Severe Dengue 
ā€¢ Recognising shock is important. Case fatality as 
high 12% 
ā€¢ Usually on day 4/5 of illness. 
ā€¢ Pulse pressure is <20mmHg 
ā€¢ Poor capillary perfusion 
ā€¢ Cold extremities 
ā€¢ Delayed cap. Refill 
ā€¢ Tachycardia 
ā€¢ Hypotension is often a late sign
6. Assessment 
ā€¢ History 
ā€¢ Important to determine timeline, family history and 
past infections in mother for infants. 
ā€¢ N.B. Maternal antibodies only protect for first 6 months. 
ā€¢ Physical Exam 
ā€¢ Vitals must be carefully observed and mental state 
ā€¢ Tourniquet test (>20 petechiae/inch2) 
ā€¢ Usu. Non-specific but maculopapular rash, 
conjunctival injection, pharyngeal oedema, 
lymphadenopathy and hepatomegaly may be seen in 
upto 50% of cases.
7. Investigations 
ā€¢ Serology: 
ā€¢ Within 3 days NS1 Strip test 
ā€¢ > 3days IgM (Potential for false positive present for 6 days 
though) 
ā€¢ IgG will indicate secondary infection (A fourfold titre increase is 
needed) 
ā€¢ Bloods 
ā€¢ FBC- Leukopenia, Changes in HCT. 
ā€¢ PLT- <150,000 
ā€¢ Peripheral blood smear- Transformed lymphocytes 
ā€¢ Albumin- low due to extravasation 
ā€¢ Liver function tests 
ā€¢ Urine output 
ā€¢ CXR, AXR, USS- to pick up fluid accumulation
8. Differentials 
Febrile Stage 
ā€¢ Leptospirosis 
ā€¢ Measles 
ā€¢ Typhoid 
ā€¢ Malaria 
Critical Phase 
ā€¢ AFI 
ā€¢ As before 
ā€¢ Surgical 
ā€¢ Acute abdomen 
ā€¢ Upper GI Bleed 
Use the timeline to differentiate. And these factors 
favour Dengue: High fever, rash, retro-orbital pain 
thrombocytopenia, leukopenia, absence of cough, and 
absence of sore-throat.
9. Management 
Steps to take 
1. Diagnosis, and classification of phase and 
severity 
2. Deciding if to be sent home, inpatient or 
emergency referral and treatment. 
3. Disease notification
9. Management (II) 
ā€¢ Group A- Outpatient 
ā€¢ No warning signs 
ā€¢ Stable socio-economic status 
ā€¢ Group B- Inpatient 
ā€¢ Warning signs 
ā€¢ Infants 
ā€¢ Poor socio-economic situation 
ā€¢ Malnutrition, concurrent infections 
ā€¢ Group C- Emergency Inpatient 
ā€¢ Severe dengue- Plasma leakage, shock, fluid 
accumulation, severe bleeds, organ impairment.
9. Management (III) 
Group A 
ā€¢ As doctor/clinic 
ā€¢ ORS, PCT, Bedrest, Vigilance 
ā€¢ Schedule daily followups. Monitor FBC, dehydration, 
warning signs and defervescence 
ā€¢ Family advice 
ā€¢ Control fever (PCT 10-15mg/kg Q6H) 
ā€¢ Prevent dehydration 
ā€¢ Prevent spread within household 
ā€¢ Watch for warning signs as temp drops after 3-8 days.
9. Management (IV) 
Group B 
ā€¢ Admit. Assess fluid status, FBC and vitals every 4 hours 
ā€¢ Continually monitor for shock and severe dengue 
ā€¢ IV fluids- Crystalloids at 6ml/kg/hr first 2 hours and then 
reassess and drop to 2-3ml/kg/hr. Maintain urine output 
and perfusion. Usu. Will pass soon into recovery or 
severe dengue. 
ā€¢ If HCT and BP stable reduce fluids 
ā€¢ If patient worsens increase to 20ml/kg for 1 hour and 
assess. 
ā€¢ If danger signs picked up proceed to Group C 
management
9. Management (V) 
Group C- Compensated Shock 
ā€¢ Admit to PICU or NICU 
ā€¢ Obtain investigations, assess fluid status and monitor 
vitals as per ward protocol 
ā€¢ Fluid: 20ml/kg crystalloid over 1 hour and reduce to 
10ml/kg for next hour if responsive and then 2- 
3ml/kg/hr for next 6-8 hours. 
ā€¢ If not improving, change to colloid solution 10-15ml/kg 
over 1 hour. Revert to crystalloids asap 
ā€¢ Once signs of reabsorbtion seen (bradycardia, rash) taper 
fluids down to maintenance levels to prevent 
hypervolaemia.
9. Management (VI) 
Group C- Hypotensive Shock or Hemorrhagic 
ā€¢ Admit to Nice or PICU, resuscitate as before. 
ā€¢ If after colloids patient still deteriorates (HCT, 
etc) transfusion ma be necessary, if HCT drops 
sharply. 
ā€¢ 5-10ml whole blood slowly over 2-4 hours and 
monitor HCT. 
ā€¢ Avoid IM injections and movement to prevent 
further bleeding
9. Management (VII) 
Fluid Overload 
ā€¢ Signs 
ā€¢ Resp. distress 
ā€¢ Cyanosis 
ā€¢ Ascitis 
ā€¢ Periorbital or soft tissue oedema 
ā€¢ Treatment 
ā€¢ Inotropic agents may be needed with small colloid 
boluses. Avoid diuretics 
ā€¢ Aspirating large effusions 
ā€¢ PPV before pulmonary oedema develops
9. Management (VIII) 
Discharge Criteria 
ā€¢ Clinically 
ā€¢ No fever for 48 hours 
ā€¢ Gen. well-being, appetite, hemodynamic status, urine 
output all improved and no respiratory distress 
ā€¢ Labs 
ā€¢ Increasing trend of platelets 
ā€¢ Stable HCT without intravenous fluids.
10. Additional Points 
ā€¢ Atypical presentations make for worse prognosis . 
ā€¢ Interestingly, the latest outbreak in Fiji saw a rise in Guillain- 
Barre syndrome. Currently under investigation. 
ā€¢ Children with suspected dengue can deteriorate very fast and 
a high index of suspicion is needed on our part. 
ā€¢ Plasma leakage is the most specific and life-threatening 
feature of severe dengue. Watch for the critical period 
carefully (Deferevescence) and donā€™t overload with fluid. 
ā€¢ Primary prevention is the way out as vaccines are not 
approved yet. Commedā€™s important afterall! ļŠ
11. References 
ā€¢ Medscape 
ā€¢ Up-to-Date 
ā€¢ WHO Publication 
ā€¢ Dengue Case Management 
ā€¢ CWM ED CME Presentation 
ā€¢ Journal articles 
ā€¢ Tropical Medicine and Intā€™ Health (2001, 2004) 
ā€¢ Indian Journal of Pediatrics (2006) 
ā€¢ Clinical Microbiology Review (2009) 
The End

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Dengue fever in Children

  • 1. Dengue Fever Jasmial Nand Paediatrics 2014
  • 2. Outline 1. References 2. Introduction 3. Pathogenesis 4. Classification 5. Clinical Course 6. Assessment 7. Investigations 8. Differentials 9. Management 10. Additional Points 11. References
  • 3. 1. References ā€¢ Medscape ā€¢ Up-to-Date ā€¢ WHO Publication ā€¢ Dengue Case Management ā€¢ CWM ED CME Presentation ā€¢ Journal articles ā€¢ Tropical Medicine and Intā€™ Health (2001, 2004) ā€¢ Indian Journal of Pediatrics (2006) ā€¢ Clinical Microbiology Review (2009)
  • 4. 2. Introduction ā€¢ The most common arbovirus globally ā€¢ Tropics at risk (approx. 2.5-3 Billion) ā€¢ 4 distinct serotypes (1-4) ā€¢ Flavivirus (ss RNA) ā€¢ Vector-borne (Genus Aedes) but other routes possible ā€¢ Common species are aegypti, albopictus and polynesiensis. ā€¢ Transmission/ Outbreak patterns ā€¢ Usually self limiting, MR <1%,
  • 5. 3. Pathogenesis Martina B E E et al. Clin. Microbiol. Rev. 2009;22:564-581
  • 6. 4. Classification Infection Asymptomatic Symptomatic Undifferentiated Dengue Fever NO Warning Signs Severe Dengue With Warning Signs 50-90%
  • 7. 4. Classification (II) ā€¢ Dengue fever without warning signs ā€¢ Hx of being in endemic area. ā€¢ Fever and 2 of the following ā€¢ Aches and pains ā€¢ Nausea & vomitting ā€¢ Rash ā€¢ Tourniquet test positive ā€¢ Leukopenia
  • 8. 4. Classification (III) ā€¢ Dengue with Warning signs ā€¢ Fluid accumulation clinically (ascitis, pleural effusion) ā€¢ Liver enlargement ā€¢ Lethargy (or restlessness) ā€¢ Lab (High HCT &/or Low PLT) ā€¢ Abdominal pain (or tenderness) ā€¢ Vomiting (persistent) ā€¢ Insignificant bleeding (Mucosal bleeding) ā€œFlaviā€
  • 9. 4. Classifications (IV) ā€¢ Severe Dengue 1. Severe plasma leakage leading to ā€¢ Shock ā€¢ Fluid accumulation with respiratory distress 2. Severe bleeding as evidenced by a doctor 3. Severe organ involvement ā€¢ Liver: AST or ALT >1000 ā€¢ CNS: Impaired consciousness ā€¢ Heart and other organ dysfunctions
  • 10. 5. Clinical Course ā€¢ Incubation period (3-7 days) ā€¢ Febrile phase (2-7 days) ā€¢ Critical phase (1-3 days) ā€¢ Marked by defervescence , leukopenia and thrombocytopenia. ā€¢ Recovery phase (or Severe Dengue.) ā€¢ May have bradycardia. Important to avoid fluid overload! ā€¢ Patients can and will present in any of the 3 stages so good history and timeline is critical to know where the patient stands and what to expect next.
  • 11. 5. Clinical Course (II) ā€¢ Severe Dengue ā€¢ Recognising shock is important. Case fatality as high 12% ā€¢ Usually on day 4/5 of illness. ā€¢ Pulse pressure is <20mmHg ā€¢ Poor capillary perfusion ā€¢ Cold extremities ā€¢ Delayed cap. Refill ā€¢ Tachycardia ā€¢ Hypotension is often a late sign
  • 12. 6. Assessment ā€¢ History ā€¢ Important to determine timeline, family history and past infections in mother for infants. ā€¢ N.B. Maternal antibodies only protect for first 6 months. ā€¢ Physical Exam ā€¢ Vitals must be carefully observed and mental state ā€¢ Tourniquet test (>20 petechiae/inch2) ā€¢ Usu. Non-specific but maculopapular rash, conjunctival injection, pharyngeal oedema, lymphadenopathy and hepatomegaly may be seen in upto 50% of cases.
  • 13. 7. Investigations ā€¢ Serology: ā€¢ Within 3 days NS1 Strip test ā€¢ > 3days IgM (Potential for false positive present for 6 days though) ā€¢ IgG will indicate secondary infection (A fourfold titre increase is needed) ā€¢ Bloods ā€¢ FBC- Leukopenia, Changes in HCT. ā€¢ PLT- <150,000 ā€¢ Peripheral blood smear- Transformed lymphocytes ā€¢ Albumin- low due to extravasation ā€¢ Liver function tests ā€¢ Urine output ā€¢ CXR, AXR, USS- to pick up fluid accumulation
  • 14. 8. Differentials Febrile Stage ā€¢ Leptospirosis ā€¢ Measles ā€¢ Typhoid ā€¢ Malaria Critical Phase ā€¢ AFI ā€¢ As before ā€¢ Surgical ā€¢ Acute abdomen ā€¢ Upper GI Bleed Use the timeline to differentiate. And these factors favour Dengue: High fever, rash, retro-orbital pain thrombocytopenia, leukopenia, absence of cough, and absence of sore-throat.
  • 15. 9. Management Steps to take 1. Diagnosis, and classification of phase and severity 2. Deciding if to be sent home, inpatient or emergency referral and treatment. 3. Disease notification
  • 16. 9. Management (II) ā€¢ Group A- Outpatient ā€¢ No warning signs ā€¢ Stable socio-economic status ā€¢ Group B- Inpatient ā€¢ Warning signs ā€¢ Infants ā€¢ Poor socio-economic situation ā€¢ Malnutrition, concurrent infections ā€¢ Group C- Emergency Inpatient ā€¢ Severe dengue- Plasma leakage, shock, fluid accumulation, severe bleeds, organ impairment.
  • 17. 9. Management (III) Group A ā€¢ As doctor/clinic ā€¢ ORS, PCT, Bedrest, Vigilance ā€¢ Schedule daily followups. Monitor FBC, dehydration, warning signs and defervescence ā€¢ Family advice ā€¢ Control fever (PCT 10-15mg/kg Q6H) ā€¢ Prevent dehydration ā€¢ Prevent spread within household ā€¢ Watch for warning signs as temp drops after 3-8 days.
  • 18. 9. Management (IV) Group B ā€¢ Admit. Assess fluid status, FBC and vitals every 4 hours ā€¢ Continually monitor for shock and severe dengue ā€¢ IV fluids- Crystalloids at 6ml/kg/hr first 2 hours and then reassess and drop to 2-3ml/kg/hr. Maintain urine output and perfusion. Usu. Will pass soon into recovery or severe dengue. ā€¢ If HCT and BP stable reduce fluids ā€¢ If patient worsens increase to 20ml/kg for 1 hour and assess. ā€¢ If danger signs picked up proceed to Group C management
  • 19. 9. Management (V) Group C- Compensated Shock ā€¢ Admit to PICU or NICU ā€¢ Obtain investigations, assess fluid status and monitor vitals as per ward protocol ā€¢ Fluid: 20ml/kg crystalloid over 1 hour and reduce to 10ml/kg for next hour if responsive and then 2- 3ml/kg/hr for next 6-8 hours. ā€¢ If not improving, change to colloid solution 10-15ml/kg over 1 hour. Revert to crystalloids asap ā€¢ Once signs of reabsorbtion seen (bradycardia, rash) taper fluids down to maintenance levels to prevent hypervolaemia.
  • 20. 9. Management (VI) Group C- Hypotensive Shock or Hemorrhagic ā€¢ Admit to Nice or PICU, resuscitate as before. ā€¢ If after colloids patient still deteriorates (HCT, etc) transfusion ma be necessary, if HCT drops sharply. ā€¢ 5-10ml whole blood slowly over 2-4 hours and monitor HCT. ā€¢ Avoid IM injections and movement to prevent further bleeding
  • 21. 9. Management (VII) Fluid Overload ā€¢ Signs ā€¢ Resp. distress ā€¢ Cyanosis ā€¢ Ascitis ā€¢ Periorbital or soft tissue oedema ā€¢ Treatment ā€¢ Inotropic agents may be needed with small colloid boluses. Avoid diuretics ā€¢ Aspirating large effusions ā€¢ PPV before pulmonary oedema develops
  • 22. 9. Management (VIII) Discharge Criteria ā€¢ Clinically ā€¢ No fever for 48 hours ā€¢ Gen. well-being, appetite, hemodynamic status, urine output all improved and no respiratory distress ā€¢ Labs ā€¢ Increasing trend of platelets ā€¢ Stable HCT without intravenous fluids.
  • 23. 10. Additional Points ā€¢ Atypical presentations make for worse prognosis . ā€¢ Interestingly, the latest outbreak in Fiji saw a rise in Guillain- Barre syndrome. Currently under investigation. ā€¢ Children with suspected dengue can deteriorate very fast and a high index of suspicion is needed on our part. ā€¢ Plasma leakage is the most specific and life-threatening feature of severe dengue. Watch for the critical period carefully (Deferevescence) and donā€™t overload with fluid. ā€¢ Primary prevention is the way out as vaccines are not approved yet. Commedā€™s important afterall! ļŠ
  • 24. 11. References ā€¢ Medscape ā€¢ Up-to-Date ā€¢ WHO Publication ā€¢ Dengue Case Management ā€¢ CWM ED CME Presentation ā€¢ Journal articles ā€¢ Tropical Medicine and Intā€™ Health (2001, 2004) ā€¢ Indian Journal of Pediatrics (2006) ā€¢ Clinical Microbiology Review (2009) The End

Editor's Notes

  1. After an incubation period of 2 to 7 days, the typical patient experiences the sudden onset of fever, headache, retroorbital pain, and back pain along with the severe myalgia that gave rise to the colloquial designation "break-bone fever." There is often a macular rash on the first day as well as adenopathy, palatal vesicles, and scleral injection. The illness may last a week, with additional symptoms usually including anorexia, nausea or vomiting, marked cutaneous hypersensitivity, and ā€” near the time of defervescence ā€” a maculopapular rash beginning on the trunk and spreading to the extremities and head.